Direct-to-consumer laboratory testing (DTCT): challenges and implications for specialists in laboratory medicine

Author:

Orth Matthias12ORCID,Vollebregt Erik3,Trenti Tomaso4,Shih Patti5,Tollanes Mette67,Sandberg Sverre6

Affiliation:

1. Vinzenz von Paul Kliniken gGmbH , Institut für Laboratoriumsmedizin , Stuttgart , Germany

2. Medizinische Fakultät Mannheim , Ruprecht Karls Universität , Mannheim , Germany

3. Axon Lawyers , Amsterdam , The Netherlands

4. Dipartimento Integrato Interaziendale di Medicina di Laboratorio e Anatomia Patologica , Azienda Ospedaliera Universitaria e Azienda USL di Modena , Modena , Italy

5. Australian Centre for Health Engagement Evidence and Values (ACHEEV), School of Health and Society , University of Wollongong NSW , Wollongong , Australia

6. Norwegian Organisation for Quality Improvement of Laboratory Examinations (NOKLUS) , Bergen , Norway

7. Global Public Health and Primary Care , University of Bergen , Bergen , Norway

Abstract

Abstract In vitro diagnostics (IVD) testing is a powerful tool for medical diagnosis, and patients‘ safety is guaranteed by a complex system of personnel qualification of the specialist in laboratory medicine, of process control, and legal restrictions in healthcare, most of them under national regulation. Direct-to-consumer laboratory testing (DTCT) is testing ordered by the consumer and performed either by the consumer at home or analysis of self-collected samples in a laboratory. However, since DTCT are not always subject to effective competent authority oversight, DTCT may pose risks to lay persons using and relying on it for healthcare decision-making. Laboratory medicine specialists should be very cautious when new DTCTs are introduced. As qualified professionals, they should feel obliged to warn and educate patients and the public about the risks of inappropriate and harmful DTCT.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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